Flavonoids from the genus Euphorbia : isolation, structure, pharmacological activities and structure–activity relationships

dc.contributor.authorMagozwi, Douglas Kemboi
dc.contributor.authorDinala, Mmabatho
dc.contributor.authorMokwana, Nthabiseng
dc.contributor.authorSiwe-Noundou, Xavier
dc.contributor.authorKrause, Rui W. M.
dc.contributor.authorSonopo, Molahlehi
dc.contributor.authorMcGaw, Lyndy Joy
dc.contributor.authorAugustyn, Wilma A.
dc.contributor.authorTembu, Vuyelwa Jacqueline
dc.date.accessioned2022-02-28T06:51:05Z
dc.date.available2022-02-28T06:51:05Z
dc.date.issued2021-05
dc.description.abstractPlants of the genus Euphorbia are widely distributed across temperate, tropical and subtropical regions of South America, Asia and Africa with established Ayurvedic, Chinese and Malay ethnomedical records. The present review reports the isolation, occurrence, phytochemistry, biological properties, therapeutic potential and structure–activity relationship of Euphorbia flavonoids for the period covering 2000–2020, while identifying potential areas for future studies aimed at development of new therapeutic agents from these plants. The findings suggest that the extracts and isolated flavonoids possess anticancer, antiproliferative, antimalarial, antibacterial, anti-venom, anti-inflammatory, anti-hepatitis and antioxidant properties and have different mechanisms of action against cancer cells. Of the investigated species, over 80 different types of flavonoids have been isolated to date. Most of the isolated flavonoids were flavonols and comprised simple O-substitution patterns, C-methylation and prenylation. Others had a glycoside, glycosidic linkages and a carbohydrate attached at either C-3 or C-7, and were designated as D-glucose, L-rhamnose or glucorhamnose. The structure–activity relationship studies showed that methylation of the hydroxyl groups on C-3 or C-7 reduces the activities while glycosylation loses the activity and that the parent skeletal structure is essential in retaining the activity. These constituents can therefore offer potential alternative scaffolds towards development of new Euphorbia-based therapeutic agents.en_ZA
dc.description.departmentParaclinical Sciencesen_ZA
dc.description.librarianpm2022en_ZA
dc.description.sponsorshipNRF-TWAS, South Africa, National Research Foundation Research and Tshwane University of Technology, Pretoria, South Africa.en_ZA
dc.description.urihttp://www.mdpi.com/journal/pharmaceuticalsen_ZA
dc.identifier.citationMagozwi, D.K.; Dinala, M.; Mokwana, N.; Siwe-Noundou, X.; Krause, R.W.M.; Sonopo, M.; McGaw, L.J.; Augustyn, W.A.; Tembu, V.J. Flavonoids from the Genus Euphorbia: Isolation, Structure, Pharmacological Activities and Structure–Activity Relationships. Pharmaceuticals 2021, 14, 428. https://doi.org/10.3390/ph14050428.en_ZA
dc.identifier.issn1424-8247 (online)
dc.identifier.other10.3390/ ph14050428
dc.identifier.urihttp://hdl.handle.net/2263/84247
dc.language.isoenen_ZA
dc.publisherMDPIen_ZA
dc.rights© 2021 by the authors. Licensee: MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/).en_ZA
dc.subjectEuphorbiaen_ZA
dc.subjectFlavonoidsen_ZA
dc.subjectPharmacological activitiesen_ZA
dc.subjectStructure–activity relationshipen_ZA
dc.subject.otherVeterinary science articles SDG-03en_ZA
dc.subject.otherSDG-03: Good health and well-being
dc.titleFlavonoids from the genus Euphorbia : isolation, structure, pharmacological activities and structure–activity relationshipsen_ZA
dc.typeArticleen_ZA

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